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. 2019 Nov 11;9:16461. doi: 10.1038/s41598-019-52839-6

Figure 2.

Figure 2

Role of nitric oxide and oxidative stress on ET-1-induced potentiation of phenylephrine response in MRA from hypertensive rats. (a) Effect of 0.1 mM L-NAME on the concentration-response curve to phenylephrine (Phe) in control and ET-1-incubated (1 nM, 90 min) segments from SHR; *P < 0.05 by two-way ANOVA with repeated measures followed by Sidak post hoc test. Differences of the AUC (dAUC) to Phe in the presence and the absence of L-NAME are also shown; *P < 0.05 by Student's t test. (b) Effect of ET-1 on eNOS mRNA levels in vascular segments; statistical analysis by Student's t test. (c) Quantification of nitric oxide (NO) release and (d) NADPH oxidase activity in control and ET-1-incubated segments from SHR; statistical analysis by Student’s t test. (e) Effect of 0.5 µM ML-171 on the concentration-response curve to Phe in control and ET-1-incubated segments from SHR; *P < 0.05 by two-way ANOVA with repeated measures followed by Sidak post-test. (f) Effect of ET-1 and L-NAME on the concentration-response curve to acetylcholine (ACh) in segments from SHR; *P < 0.05 vs Control; #P < 0.05 vs ET-1 by two-way ANOVA with repeated measures followed by Sidak post hoc test. (g) Quantification of ACh-induced NO release in control and ET-1-incubated segments from SHR; statistical analysis by Student's t test. n denotes number of experiments.